Show 5 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="VAN REGEMORTER, N" or (type exact bookEditor and editor="VAN REGEMORTER, N") Add to list Journal Article A2 Further evidence for a recessive form of SEMD resembling pseudoachondroplasia in a consanguineous family of Maghrebian origin D Anrom, N Van Regemorter, Y Sznajer, G Jackson, M Briggs and Geert Mortier (UGent) (2008) EUROPEAN JOURNAL OF HUMAN GENETICS. 16. p.70-70 Add to list Journal Article A1 Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy J DESIR, G MOYA, O REISH, N VAN REGEMORTER, H DECONINCK, KL DAVID, Françoise Meire (UGent) and MJ ABRAMOWICZ (2007) JOURNAL OF MEDICAL GENETICS. 44(5). p.322-326 Add to list Journal Article A1 A novel mutation in the ELOVL4 gene causes autosomal dominant Stargardt-like macular dystrophy A MAUGERI, Françoise Meire (UGent) , CB HOYNG, C VINK, N VAN REGEMORTER, G KARAN, ZL YANG, FPM CREMERS and Kaibo Zhang (2004) INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE. 45(12). p.4263-4267 Add to list Journal Article A1 Delineation of two distinct 6p deletion syndromes. AF DAVIES, G MIRZA, G SEKHON, P TURNPENNY, F LEROY, Franki Speleman (UGent) , C LAW, N VAN REGEMORTER, E VAMOS, F FLINTER, et al. (1999) HUMAN GENETICS. 104(1). p.64-72